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Anti-C5 Fc Silent Antibody (CB-LX004-A)

Cat#: CB-LX004-A
Target: C5
Isotype: IgG4, Kappa
Host: Humanized

Product Type Fc Silent Antibody

Description Anti-Human C5-Fc silent antibody is a Human monoclonal antibody targeting the C5. And it is intended for the research of Autoimmune diseases.

Research Area Cell Biology, Immunology

Antigen Distribution Restricted expression toward thyroid (RPKM 13.7).

Disease Autoimmune diseases

Size 100 ug

Immunogen Recombinant Human C5 protein

Species Human

Clonality Monoclonal

Conjugation Unconjugated

Source Recombinant

Buffer PBS, pH 7.4

Application Funcs, In vivo assay

Application Notes The use of diluent depends on the detection system used. It is recommended that users test reagents and determine their own optimal dilution.

Handling Advice This product is for research use only. It is not intended for use in therapeutic or diagnostic procedures for humans or animals.

Storage Instructions Product should be stored at -80°C. Repeated freeze and thaw cycles will cause loss of activity. Use product within 24 hours after thawing and keep on ice. Remainder amounts should be aliquoted and immediately re-freezed for future use. Aliquots should never be thawed more than once. Under recommended storage conditions, product is stable for at least one year.

Official Name Complement C5

Full Name Complement C5

Background This gene encodes a component of the complement system, a part of the innate immune system that plays an important role in inflammation, host homeostasis, and host defense against pathogens. The encoded preproprotein is proteolytically processed to generate multiple protein products, including the C5 alpha chain, C5 beta chain, C5a anaphylatoxin and C5b. The C5 protein is comprised of the C5 alpha and beta chains, which are linked by a disulfide bridge. Cleavage of the alpha chain by a convertase enzyme results in the formation of the C5a anaphylatoxin, which possesses potent spasmogenic and chemotactic activity, and the C5b macromolecular cleavage product, a subunit of the membrane attack complex (MAC). Mutations in this gene cause complement component 5 deficiency, a disease characterized by recurrent bacterial infections. Alternative splicing results in multiple transcript variants.

Alternative Names Complement C5; C3 and PZP-like alpha-2-macroglobulin domain-containing protein 4; C5a anaphylatoxin; anaphylatoxin C5a analog; Complement component 5; Prepro-C5; C5Da; C5b; CPAMD4; ECLZB; C5

Gene ID 727

Uniprot ID P01031

All products and services are for Research Use Only. Do Not use in humans.

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